Your browser doesn't support javascript.
loading
MiR362-3p Alleviates Osteosarcoma by Regulating the IL6ST/JAK2/STAT3 Pathway in Vivo and in Vitro.
Hu, Yunteng; Li, Jianjun; Liu, Chun; Zhang, Xue; Wang, Yihan; Lin, Jiezhao; Peng, Ziyue; Zhu, Lixin.
Afiliação
  • Hu Y; Department of Spine Surgery, Zhujiang Hosptial, Southern Medical University, Guangzhou, China.
  • Li J; Department of Spine Surgery, Zhujiang Hosptial, Southern Medical University, Guangzhou, China.
  • Liu C; Department of Spine Surgery, Zhujiang Hosptial, Southern Medical University, Guangzhou, China.
  • Zhang X; Department of Rehabilitation Medicine, The First Affiliated Hospital of Gannan Medical College, Ganzhou, China.
  • Wang Y; Department of Spine Surgery, Zhujiang Hosptial, Southern Medical University, Guangzhou, China.
  • Lin J; Department of Spine Surgery, Zhujiang Hosptial, Southern Medical University, Guangzhou, China.
  • Peng Z; Department of Spine Surgery, Zhujiang Hosptial, Southern Medical University, Guangzhou, China.
  • Zhu L; Department of Spine Surgery, Zhujiang Hosptial, Southern Medical University, Guangzhou, China.
Technol Cancer Res Treat ; 23: 15330338241261616, 2024.
Article em En | MEDLINE | ID: mdl-39051528
ABSTRACT

Objectives:

To investigate the effects and the related signaling pathway of miR-362-3p on OS.

Methods:

The bioinformatics analysis approaches were employed to investigate the target pathway of miR-362-3p. After the 143B and U2OS cells and nu/nu male mice were randomly divided into blank control (BC) group, normal control (NC) group, and overexpression group (OG), the CCK-8, EdU staining, wound healing assay, Transwell assay, and TUNEL staining were adopted to respectively determine the effects of overexpressed miR-362-3p on the cell viability, proliferation, migration, invasion, and apoptosis of 143B and U2OS cells in vitro, tumor area assay and hematoxylin and eosin staining were employed to respectively determine the effects of overexpressed miR-362-3p on the growth and pathological injury of OS tissue in vivo. The qRT-PCR, Western blot, and immunohistochemical staining were applied to respectively investigate the effects of overexpressed miR-362-3p on the IL6ST/JAK2/STAT3 pathway in OS in vivo and in vitro.

Results:

The bioinformatics analysis approaches combined qRT-PCR indicated that the IL6ST/JAK2/STAT3 is one of the target pathways of miR-362-3p. Compared with NC, the cell viability, proliferation, migration, and invasion of 143B and U2OS cells were dramatically (P < 0.01) inhibited but the apoptosis was prominently (P <0 .0001) promoted in OG. Compared with NC, the growth of OS tissue was significantly (P < 0.05) suppressed and the pathological injury of OS tissue was substantially aggravated in OG. The gene expression levels of IL6ST, JAK2, and STAT3 and the protein expression levels of IL6ST, JAK2, p-JAK2, STAT3, and p-STAT3 in 143B and U2OS cells were memorably (P < 0.0001) lower in OG than those in NC. In addition, the positively stained areas of proteins of IL6ST, JAK2, p-JAK2, STAT3, and p-STAT3 of OS tissue in OG were markedly (P < 0.01) reduced compared with those in NC.

Conclusion:

The overexpression of miR362-3p alleviates OS by inhibiting the IL6ST/JAK2/STAT3 pathway in vivo and in vitro.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Osteossarcoma / Regulação Neoplásica da Expressão Gênica / Movimento Celular / Apoptose / MicroRNAs / Proliferação de Células / Fator de Transcrição STAT3 / Janus Quinase 2 Limite: Animals / Humans / Male Idioma: En Revista: Technol Cancer Res Treat Assunto da revista: NEOPLASIAS / TERAPEUTICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Osteossarcoma / Regulação Neoplásica da Expressão Gênica / Movimento Celular / Apoptose / MicroRNAs / Proliferação de Células / Fator de Transcrição STAT3 / Janus Quinase 2 Limite: Animals / Humans / Male Idioma: En Revista: Technol Cancer Res Treat Assunto da revista: NEOPLASIAS / TERAPEUTICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos